热重分析
金属有机骨架
聚乙二醇
吸附
环糊精
粉末衍射
扫描电子显微镜
化学工程
材料科学
核化学
化学
有机化学
结晶学
工程类
复合材料
作者
Botao Liu,Yaping He,Liping Han,Vikramjeet Singh,Xiaonan Xu,Tao Guo,Fanyue Meng,Xu Xu,Peter York,Zhaoxin Liu,Jiwen Zhang
标识
DOI:10.1021/acs.cgd.6b01658
摘要
The micron and nanometer-sized γ-cyclodextrin metal–organic frameworks (γ-CD-MOFs) were successfully synthesized using the microwave technique for the first time for rapid and facile synthesis. Polyethylene glycol 20000 (PEG 20000) was used as surfactant to control the size and morphology of γ-CD-MOFs. The as-synthesized γ-CD-MOFs were characterized using various techniques, including X-ray powder diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and N2 adsorption. The increment in the reaction time and MeOH ratio dramatically damaged the crystalline integrity of γ-CD-MOFs. Fenbufen was selected as a model drug to evaluate the loading characteristics of γ-CD-MOF crystals. As a result, the nanometer sized γ-CD-MOFs (100–300 nm) showed rapid and higher adsorption (196 mg g–1) of Fenbufen in EtOH when compared with the micron crystals. The adsorption parameters fitted well to a pseudo-second-order kinetic model and chemisorption of Fenbufen was further supported by molecular docking illustrations. In summary, the controlled synthesis of γ-CD-MOFs was successfully achieved by microwave assisted method and resultant crystals were further evaluated for potential drug delivery applications.
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